@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_head
{
this:
np:hasAssertion
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_assertion
;
np:hasProvenance
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_provenance
;
np:hasPublicationInfo
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_assertion
a
np:Assertion
.
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_provenance
a
np:Provenance
.
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0268080
a
ncit:C7057
.
dgn-gda:DGN4d13fab72810905fd1ba4eabba81890b
sio:SIO_000628
miriam-gene:7421
,
lld:C0268080
;
a
sio:SIO_001121
.
}
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_provenance
{
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_assertion
dcterms:description
"[Although the identification of mechanisms mediating VDR-regulated transcription has been one focus of recent research in the field, other topics of fundamental importance include the identification and functional significance of proteins involved in the metabolism of vitamin D. CYP2R1 has been identified as the most important 25-hydroxylase, and a critical role for CYP24A1 in humans was noted in studies showing that inactivating mutations in CYP24A1 are a probable cause of idiopathic infantile hypercalcemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:26681795
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP1295795.RA2pLY_P5SFKDJLtsHi3jhtN_ubC14Sb4HPMfGn5HBz1c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:33+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}